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Acta Cirurgica Brasileira

Print version ISSN 0102-8650On-line version ISSN 1678-2674

Acta Cir. Bras. vol.31 no.11 São Paulo Nov. 2016

http://dx.doi.org/10.1590/s0102-865020160110000002 

Original Articles

The effects of passive tobacco smoking on the microcirculation of the abdominal wall in rats1

Paulo Sandler I  

Bernardo Mastella II  

Diego Uchôa III  

Geraldo Pereira Jotz IV  

Henrique Záchia Leão V  

Leandro Totti Cavazzola VI  

IMD, Department of Surgery, Hospital de Clínicas de Porto Alegre (HCPA), Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre-RS, Brazil. Conception and design of the study, critical revision.

IIUndergraduent student, School of Medicine, HCPA, UFRGS, Porto Alegre-RS, Brazil. Acquisition, analysis and interpretation of data; technical procedures; manuscript preparation.

IIIPhD, Department of Pathology, HCPA, UFRGS, Porto Alegre-RS, Brazil. Histopathological examinations, critical revision.

IVPhD, Postgraduate Program in Health Sciences, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA). Morphological Sciences Department, UFRGS, Porto Alegre-RS, Brazil. Conception and design of the study.

VDHSc, Postgraduate Program in Health Sciences, UFCSPA. School of Medicine, Universidade Luterana do Brasil (ULBRA), Canoas-RS. Morphological Sciences Department, UFRGS, Porto Alegre-RS, Brazil. Conception and design of the study.

VIPhD, Department of Surgery, Hospital de Clínicas de Porto Alegre (HCPA), Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre-RS, Brazil. Scientific, intellectual, conception and design of the study; analysis and interpretation of data, critical revision, final approval.


ABSTRACT

PURPOSE:

To analysis the effects of passive smoking on the microstructure of tissues of the abdominal wall regarding microcirculation, using histopathological study of the tobacco exposed rats.

METHODS:

Twenty four male Wistar rats were divided in Control Group (CG = 8 animals) and Exposition Groups (EG = 16 animals). EG was exposed to cigarette smoke 4x/day for 120 days, while CG was preserved from exposure. Food, water and housing were similar for both groups. After 120 days, urine samples were collected before necropsy to analyze cotinine levels (ng/mL) in urine and blinded histopathological analysis of the abdominal wall performed to count arteries and veins in dermal and muscular fascia layer.

RESULTS:

No difference in weight was observed between both groups (P>0.05). Cotinine concentration was significantly higher in EG (P<0.05). In dermal layer, the average of vessels per animal was 8.72 (IC95%: 8.31-9.13) for CG and 11,23 (IC95%: 10.09-12.38) for EG. In muscular fascia layer the average of vessels per animal was 17.97 (IC95%: 15.79-20.15) for CG, whereas the average for EG was of 14,85 (IC95%: 12.71-17.01) (P<0.05).

CONCLUSION:

Exposition to passive smoking may cause increase in the number of vessels in dermal layer, with the opposite effects at the muscular fascia layer.

Key words: Tobacco Products; Abdominal Wall; Smoke Inhalation Injury; Physiopathology; Rats

Introduction

The role of cigarette smoking is well established for many diseases, making this habit the leading cause of preventable death in the world1.

There are many clinical trials and meta-analyses showing that smokers who underwent surgical events had more post operatory complications comparing to non smokers or smokers who had a bigger cessation time before and after surgery1-4.

Studies suggest that the products of cigarette smoke may cause changes in the microstructure of tissues secondary to microcirculatory deficiency, oxygen concentration, tissue healing mechanisms, inflammatory process and others. This could predispose one who is undergoing surgery to complications such as infections, necrosis, delayed or anomalous wound healing, incisional hernia, among others4-6. Black et al.7 used human skin grafts to show that the presence of short-term nicotine amplified the concentration-dependent dermal vasoconstrictor effect of norepinephrine (NE) and attenuated endothelium-dependent skin vasorelaxation induced by acetylcholine in NE-preconstricted skin vasculature, without affecting endothelium-independent vasorelaxation induced by nitroglycerine in NE-preconstricted dermal vasculature. Similar results were reaffirmed by Ijzerman et al.8.

Among the postoperative complications in abdominal wall surgery, the wound infection is one of the most feared, as it changes the normal recovery of tissue layers, leading to occurrence of incisional hernia in almost 50% of its cases, generating augmented costs, number of hospital readmissions and hospital stay9,10.

Dermal and subcutaneous tissue infections are clearly associated with the presence of ischemia of the skin layers involved11-13. Kool et al.14 states that cigarette smoking, apart from increasing systemic blood pressure and heart rate, also reduces dermal circulation when in short-term.

In the present study, the effects of cigarette smoke products in the microstructure of the tissues of the abdominal wall will be assessed regarding its microcirculation.

Methods

The present study was approved by the Ethics Committee on Animal Use (CEUA) of the Universidade Federal do Rio Grande do Sul (UFRGS), under protocol nº 19.127 and the Ethics Committee on Animal Use on Animal Use (CEUA) of the Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA).

Twenty-four male Wistar rats (Rattus norvegicus) were randomly divided into two groups: Exposition Group (EG = 16 animals) and Control Group (CG = 8 animals). The number of animals for this type of experiment has been statistically validated. The exposure of the animals to passive cigarette smoke was induced according to previous experimental protocols, as it follows15-17.

The animals in EG were placed in plastic boxes, measuring approximately 30x40 cm³ (four per box), with a wire mesh platform to access food and water. The boxes containing the animals were transferred to a laminar flow hood (CQ 800, Union Equipment Laboratorial(r)), measuring 60 cm x 80 cm, with a 20 cm x 20 cm pyramid-shaped exhaust type18.

The concentration of CO in the exhaust hood was adjusted according to previous protocols (CO concentration between 100-130 ppm). The hood had a single overhead outlet and the airflow was passive, with an average temperature of 22 °C and average umidity of 60%.

The concentration of particulate smoke was measured with a nephelometer (DustTrakII(r), model 8532, serial number 8.53E+09), with a tube including a 2.4 µg/m3 /per minute air filter. This device was used from five minutes after onset of exposure until cycle completion.

Over a period of 120 days, from the 12th after birth, the animals were exposed daily to the smoke generated by 16 lit cigarettes (four cigarettes in each session, with four sessions a day, at 8h, 12h, 16h and 20h). Each session lasted 20 minutes, while cigarette combustion lasted 10 minutes on average. When not in sessions, the animals which had not yet been weaned were placed together with their mothers.

The smoke was administred in the absence of the mother until the pups were weaned (at 21 days), to avoid contaminating the breast milk. During exposure, the boxes containing EG were transferred to a laminar flow hood with four cigarettes in combustion. The ambient smoke (inside the hood) dissipated passively through the extract vent on the exterior. We used commercial filter cigarettes with the following composition: 10 mg of tar, 0,8 mg nicotine and 10 mg carbon monoxide.

The animals from CG were housed in two open boxes in the same room as the animals exposed to secondhand smoke, 5 meters away from the hood. The animals from both groups had free access to water and food.

Analysis of cotinine levels

Exposure of animals to cigarette smoke was assessed by urinary concentrations of cotininte (biomarker of tobacco passive consumption). Urine samples were collected at the end of exposure (120 days) by suprapubic aspiration while the animals were under anesthesia, immediately before euthanasia. The cotinine levels were quantified using high performance liquid chromatography (HPLC) according to the protocol established by Ceppa et al.19. Necropsy: After 120 of exposure, following all the protocols required by Resolution nº 1000 of the Federal Council of Veterinary Medicine, all animals suffered euthanasia using the appropriate intraperitoneal dose of ketamine (75-90 mg/kg)18 and xylazine (10 mg/kg), with injection of 1000 IU of heparine (Cristália, Brazil) at the left ventricle of the heart. Using a peristaltic pump, the animals were perfused with 200 mL of saline solution, followed by 200 mL of 4% paraformaldehyde (Reagan, Brazil) diluted in phosphate 0.1M "buffer" solution (pH 7,4, PBS), at room temperature.

Histological processing

Two fragments of abdominal wall were removed. The fragments removed should contain all layers of the abdominal wall, from peritoneum to epidermal layer, and measure about 4.0 cm². Next, the samples were fixed in 10% buffered formalin and later processed and embedded in paraffin. From paraffin blocks, 4.0 µm thick sections were cut using a microtome (Leitz), then deparaffinized. Histological sections were then stained using hematoxylin and eosin technique (H & E). The slides were examined using an Olympus BX41 microscope (Japan), together with an Olympus DP73 camera (Japan).

The fragments were carefully placed in paraffin and cut transversely in relation to the abdominal wall to allow the simultaneous microscopic observation of all tissue layers of the abdominal wall from skin to peritoneum. Thus, all possible histopathological changes in each layer can be described separately, such as edema, hyperemia, acute inflammation, chronic inflammation, angiogenesis foci, hyperplasia, atrophy, degeneration and pigmentation changes.

Pathological analysis

The vessel counting was performed by an experienced pathologist, blinded in relation to the study groups, who randomly selected four high-power fields (x400) of each area to be studied in each section (Figure 1). In each high-power field a vessel counting was performed separately, yielding four different counts. Arterioles were not considered separatedely, and therefore were counted along with veins.

FIGURE 1 Histological analysis of the abdominal walls of some of the animals used in the study (HE staining). The images illustrate the method used to define the exploited area, in increments of 12.5x (1), x40 (2), x100 in the fascia area and derma (3 and 4, respectively) and x400 in the region of fascia and dermis (5 and 6, respectively). Random areas were selected at x400 of the laminas, in both regions, to perform the vessel counting (arrows). Key A: derma region; Key B: Hipoderma; Key C: panniculus carnosus; Key D: Fascia; Key E: muscle of the abdominal wall; Asterisks: artifact region between the fabric layers. 

This four high-power fields counting was conducted in two distinct areas of the abdominal wall: one at the dermal layer and another one next to muscular fascia. Thus, each animal, both in the control group as in the exposure group, received two separate counts.

Statistical analysis

A Poisson regression was performed in order to compare differences in vessel numbers in two groups of animals for both dermis and fascia. Thus, each animal studied received two separated countings, both in the control group as in the exposure group.

Results

At the end of the experiment the analysis of animal weight showed no significant differences between EG (376.4+52.8 g) and CG (363.2+35.8 g) (P = 0.532). Moreover, analysis of the urinary cotinine concentration in the rats from the EG (4.72+0.89 ng/ml) was significantly higher than the concentration in CG (0.65+0.12 ng/ml) (P = 0.0001).

Exposure to the particulate smoke, measured by the nephelometer, showed an average exposure of 98.4 µg/m3, between the sixth and tenth minute of exposure, 86.6 µg/m3, between the eleventh and fifteenth minute of exposure and an abrupt fall to 2.8 µg/m3 in the last five minutes of exposure.

In the layer of the dermis (Figure 2), the average number of vessels per animal was 8.72 (95% CI: 8.31 - 9.13) in CG and 11.23 (95% CI: 10.09 - 12.38) in EG (P <0.05).

FIGURE 2 Graphic showing the average of vessel counting at dermal layer, divided by groups (CG and EG). The average of vessel counting for EG is statistically superior than the average of vessel counting for CG for this tissue layer. 

In the layer of fascia (Figure 3), CG showed an average of 17.97 (95% CI: 15.79 - 20.15) vessels, while EG showed an average of 14.85 (95% CI: 12.71 - 17.01) vessels in the same region (P <0.05).

FIGURE 3 Graphic showing the average of vessel counting at fascial layer, divided by groups (CG and EG). The average of vessel counting for EG is statistically superior than the average of vessel counting for CG for this tissue layer. 

Discussion

The relationship between cigarette smoking and post-operative complications is well established in the literature, such as infection of surgical wound (SW), graft necrosis or incisional hernias2-5,20. Soresen et al.21 reports that smoking is associated with SW infection at all types of surgery, with an odds ratio (OR) of 2,95 for SW infections in light smokers and an OR of 3,46 for heavy smokers. A similar association was found regarding skin flap necrosis and epidermolysis after simple mastectomy and modified radical mastectomy. Patients who smoked until the date of the surgery compared to nonsmoker patients or smokers who started using nicotine patches or placebo prior to the surgery. On the other hand, a short period of abstinence is sufficient to reduce the risk of infection22.

Among the mechanisms affected by cigarette smoking that lead to disorders in wound repair, we can point to decreased blood flow by vasoconstriction in small cutaneous vessels.

Several studies have pointed out this phenomenon in cutaneous circulation, either by Doppler ecography of smokers4 or by flow study of skin flaps12. As a result, the tissue oxygenation and aerobic metabolism will be adversely affected12.

The hypoxia caused by this decreased flow is identified as a major trigger for the transcription of angiogenic factors22,23, including the hypoxia-induced factor 1 (HIF-1). This transcription factor, as expressed by its name, is induced by low oxygen tension. HIF-1 is degraded under normal oxygen concentrations, but stabilized in low concentrations, activating the transcription of several genes, including vascular endothelial growth factor (VEGF) and flt-1, its receptor.

Morimoto et al.24 demonstrated, using animal models, that the use of nicotine at low concentrations, such as those released in patches, is associated with significantly greater repairs in the same time period than their respective controls that were not exposed to any substance. However, higher levels of nicotine, similar to those obtained with the use of cigarettes, showed a poorer wound healing comparing to control.

Based on previously established review, it appears that our findings are supported by the literature. Knowing that the cigarette has a pivotal role in wound healing dysfunction, our previously expectations before analyzing the data was that the number of vessels would be decreased in the EG in relation to our control, both in dermis and fascia. However, the findings in dermal layer pointed in the opposite direction to show a higher average of vessels in animals exposed to smoke than their control peers.

From this observation, we speculate that this finding may be the result of the effects of hypoxia and products they originate, as the HIF-1. In addition, the angiogenic effects of nicotine, which occur by stimulation of nicotinic acetylcholine receptors25,26 can be concurrent responsible for this significant increase in the amount of exposed vessels in the dermis layer.

To interpret this finding based on what is known from literature about the relationship of cigarette and wound healing, one can conjecture that cigarette smoking increases the number of vessels as an adaptation to a state of hypoxia by chronic exposure to smoking. However, as this is a post mortem analysis of a healthy tissue, it is suggested that although angiogenesis occurs, it is not the determining factor for a proper healing, probably because it is not able to completely restore normal oxygen tension. Other consequences of tobacco use should lead to a poor healing even with increased vascularization.

From the best of our knowledge, our study is the first one to analyze angiogenesis and cigarette smoking by direct vessel counting in dermal and muscular fascia layer. Other studies used other kinds of biomarkers that support our findings, even though do not use the same method. Morimoto et al.24, uses immunohistological staining of von Willebrand to analyze newly formed capillaries in the wound bed of its rats. Heeschen et al.25 stated that nicotine at low concentrations promotes arteriogenesis using capillary density.

Some of the findings of this study however remain unclarified. As the number of vessels in the dermal layer is significantly greater in EG, the fascia also has shown significant difference to an opposite direction. The literature research made for this study has not found any explanation for this finding, nor any evidence that this could lead to poor wound healing. Further studies are necessary to determine the quality of this angiogenesis in the exposed animals, to evaluate if this response restores tissue vascularization properly.

Even so, this study contributes to the understanding of the phenomena consequent on the use of cigarette, contributing to the knowledge about its effects on regeneration and wound healing.

Conclusions

Histopathological analysis of abdominal wall of Wistar male rats exposed to passive cigarette smoke showed an increased number of vessels in dermal layer and a decreased number in vessels of muscular fascia layer when compared to control rats.

Although we have not found any other study that used the same vessel counting analysis as we did to compare the results, many other ways to assess microvasculature corroborates with our findings. Our findings may show an impaired vascular response to ischemic effects caused by nicotine, unable to restore normal blood flow, which ultimately could lead to impairments in surgical wound repair.

Acknowledgements

To Antonio Generoso Severino, and Clovis Tadeu Bevilacqua Filho for their technical assistance; the students Cilomar Martins de Oliveira Filho, Pedro Henrique Duarte Marks, and Victor Hugo Vargas Bittencourt for the help during the experiments.

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Financial source: none

1Research performed at Basic Health Sciences Institute (ICBS), Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre-RS, Brazil. Part of Master degree thesis, Postgraduate Program in Surgery, UFRGS. Tutor: Leandro Totti Cavazzola.

Received: July 18, 2016; Revised: September 19, 2016; Accepted: October 17, 2016

Correspondence: Leandro Totti Cavazzola Departamento de Cirurgia, Hospital de Clínicas de Porto Alegre Universidade Federal do Rio Grande do Sul Rua Ramiro Barcelos, 2350 90035-903 Porto Alegre - RS Brasil cavazzola@gmail.com cavazzola@hotmail.com

Conflict of interest:

none

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